Didanosine

Product NDC

0555-0588

11-digit product format

005550588

Labeler code

0555

Product ID

0555-0588_26a65fcc-62e2-4807-aa52-5bd5cbd6389e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Didanosine

Dosage form

CAPSULE, DELAYED RELEASE PELLETS

Route

ORAL

Labeler

Teva Pharmaceuticals USA,

Application

ANDA077167

Marketing category

ANDA

Marketing start

2004-12-15

Marketing end

2019-03-31

Substance

DIDANOSINE

Active strength

200 mg/1

Pharmacologic classes

Human Immunodef

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record